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REGULATED INFORMATION Nyxoah Reports First Quarter 2022 Financial and Operating Results Mont-Saint-Guibert, Belgium

Key Takeaway: First Quarter 2022 Financial and Operating Results Belgium - May 10, 2022, 08:50pm CET / 2:50pm ET - Nyxoah SA (Euronext Brussels/Nasdaq: NYXH) ("Nyxoah" or the "Company"), a medical technology company focused on the development and commercialization of innovative solutions to

Full Press Release Details

First Quarter 2022 Financial and Operating Results
Belgium - May 10, 2022, 08:50pm CET / 2:50pm ET - Nyxoah SA (Euronext Brussels/Nasdaq: NYXH) ("Nyxoah"
or the "Company"), a medical technology company focused on the development and commercialization of innovative solutions to
treat Obstructive Sleep Apnea (OSA), today reported financial and operating results for the first quarter of 2022.
First Quarter 2022 Financial and Operating
"I am extremely pleased with our first quarter
results and strong execution that resulted in an acceleration in sales and DREAM implants as we progress towards achieving all of our
strategic priorities for 2022 and beyond," commented Olivier Taelman, Nyxoah's Chief Executive Officer. "On the commercial
side, the 660,000 of revenue we booked in the first quarter was roughly equal to the revenue performance from the previous three
quarters combined. We now have 15 active implant sites in Germany, and we will continue to add 10 more sites by the end of the third quarter.
This growth validates our patient-centric, Going Deep' strategy of developing Centers of Excellence as we increase therapy
penetration at each of these sites. We were also thrilled to implant our first commercial CCC patients in Germany, and we expect continued
acceleration in CCC implants following the positive response to our BETTER SLEEP data presentation at the World Sleep Congress in Rome,
where we hosted 55 key opinion leaders during the pre-Congress symposium."
Mr. Taelman continued, "We are also
happy with the acceleration in the pace of implants in our DREAM U.S. pivotal study, given recent weekly implant rates, which have increased
meaningfully over the last month. We believe we have enough patients enrolled to complete the study by the end of the second quarter of
2022, particularly in light of the FDA's approval to reduce the sample size to 115 patients. We also continue our dialogue with
FDA regarding our IDE submission for our ACCCESS trial for CCC patients in the U.S., and we expect to implant our first patient before
the end of this year."
"Finally, I am thrilled to announce
the nominations of Ray Cohen and Ginny Kirby for appointment to the Board of Directors. They will bring a wealth of knowledge that will
benefit Nyxoah as we complete DREAM, prepare for our U.S. launch, and advance our pipeline. I look forward to working closely with both
of them," concluded Mr. Taelman.
First Quarter 2022 Results
condensed consolidated interim financial statements as at and for the three months ended March 31, 2022 - Interim consolidated
statements of loss and other comprehensive loss (in thousands)
For the three months ended March 31
Notes 2022 2021
Revenue 660 185
Cost of goods sold (289 ) (52 )
Gross profit 371 133
Research and Development Expense (3 595 ) (3 094 )
Selling, General and Administrative Expense (4 193 ) (2 366 )
Other income/(expense) 136 4
Operating loss for the period (7 281 ) (5 323 )
Financial income 1 576 4
Financial expense (788 ) (325 )
Loss for the period before taxes (6 493 ) (5 644 )
Income taxes (208 ) (25 )
Loss for the period (6 701 ) (5 669 )
Loss attributable to equity holders (6 701 ) (5 669 )
Other comprehensive loss
Items that may be subsequently reclassified to profit or loss (net of tax)
Currency translation differences (102 ) (70 )
Total comprehensive loss for the year, net of tax (6 803 ) (5 739 )
Loss attributable to equity holders (6 803 ) (5 739 )
Basic Loss Per Share (in EUR) (0.260 ) (0.256 )
Diluted Loss Per Share (in EUR) (0.260 ) (0.256 )
The accompanying notes are an integral part
of these condensed consolidated interim financial statements
REGULATED INFORMATION
UNAUDITED CONSOLIDATED BALANCESHEET (in thousands)
As at
March 31 2022 December 31 2021
ASSETS
Non-current assets
Property, plant and equipment 2 048 2 020
Intangible assets 28 526 25 322
Right of use assets 3 154 3 218
Deferred tax asset 529 46
Other long-term receivables 165 164
34 422 30 770
Current assets
Inventory 301 346
Trade receivables 619 226
Other receivables 1 607 2 286
Other current assets 1 197 1 693
Financial assets 45 041 -
Cash and cash equivalents 82 787 135 509
131 552 140 060
Total assets 165 974 170 830
EQUITY AND LIABILITIES
Capital and reserves
Capital 4 432 4 427
Share premium 228 158 228 033
Share based payment reserve 3 788 3 127
Other comprehensive income 100 202
Retained loss (93 864 ) (87 167 )
Total equity attributable to shareholders 142 614 148 622
LIABILITIES
Non-current liabilities
Financial debt 7 952 7 802
Lease liability 2 664 2 737
Pension liability 80 80
Provisions 22 12
Deferred tax liability - 5
10 718 10 636
Current liabilities
Financial debt 598 554
Lease liability 599 582
Trade payables 3 401 3 995
Current tax liability 3 588 2 808
Other payables 4 456 3 633
12 642 11 572
Total liabilities 23 360 22 208
Total equity and liabilities 165 974 170 830
condensed consolidated interim financial statements as at and for the three months ended March 31, 2022 - Interim consolidated
statements of cash flows (in thousands)
For the three months ended March 31
2022 2021
CASH FLOWS FROM OPERATING ACTIVITIES
Loss before tax for the year (6 493 ) (5 644 )
Adjustments for
Finance income (1 576 ) (4 )
Finance expenses 788 325
Depreciation and impairment of property, plant and equipment and right-of-use assets 255 164
Amortization of intangible assets 208 211
Share-based payment transaction expense 665 -
Increase/(decrease) in provisions 10 -
Other non-cash items 180 3
Cash generated before changes in working capital (5 963 ) (4 945 )
Changes in working capital
Decrease/(Increase) in inventory 45 (51 )
(Increase)/decrease in trade and other receivables 884 (1 195 )
Increase/(Decrease) in trade and other payables (392 ) 2 170
Cash generated from changes in operations (5 426 ) (4 021 )
Interests received - 1
Income tax paid (65 ) (34 )
Net cash used in operating activities (5 491 ) (4 054 )
CASH FLOWS FROM INVESTING ACTIVITIES
Purchases of property, plant and equipment (128 ) (169 )
Capitalization of intangible assets (3 412 ) (1 606 )
(Increase)/decrease in financial assets - current (44 032 ) -
Net cash used in investing activities (47 572 ) (1 775 )
CASH FLOWS FROM FINANCING ACTIVITIES
Payment of principal portion of lease liabilities (146 ) (135 )
Repayment of other loan (21 ) (21 )
Interests paid (109 ) (105 )
Proceeds from issuance of shares, net of transaction costs 130 52
Other financial costs (2 ) -
Net cash generated from financing activities (148 ) (209 )
Movement in cash and cash equivalents (53 211 ) (6 038 )
Effect of exchange rates on cash and cash equivalents 489 (55 )
Cash and cash equivalents at January 1 135 509 92 300
Cash and cash equivalents at March 31 82 787 86 207
Revenue was 660,000 for the first quarter
ending March 31, 2022, compared to 185,000 for the first quarter ending March 31, 2021. The increase in revenue was attributable
to the Company's commercialization of the Genio system, primarily in Germany.
Cost of goods sold was 289,000 for the three
months ending March 31, 2022, representing a gross profit of 371,000, or gross margin of 56.2%.
Research and Development Expenses
Research and Development expenses were 3.6
million for the three months ending March 31, 2022, versus 3.1 million for the prior year period, reflecting the Company's
investments in the development of next generation versions of the Genio system as well as ongoing clinical studies, most
notably DREAM in the U.S.
Selling, General and Administrative Expenses
General and administrative expenses rose to 4.2
million for the first quarter of 2022, up from 2.4 million in the first quarter of 2021. This was due primarily to increased commercial
efforts in Germany and other European markets, as well as investments in Nyxoah's corporate infrastructure. The Company expects
to continue adding headcount across the organization ahead of U.S. commercial launch.
Total operating loss for the first quarter of
2022 was 7.3 million versus 5.3 million in the first quarter of 2021, driven by the acceleration in our R&D spending,
as well as ongoing commercial and clinical activities. Nyxoah realized a net loss of 6.7 million for the quarter ended March 31,
2022, compared to a net loss of 5.7 million for the quarter ended March 31, 2021.
REGULATED INFORMATION
As of March 31, 2022, cash and financial
assets totaled 127.8 million on March 31, 2022, compared to 135.5 million on December 31, 2021. Total cash burn
was approximately 2.6 million per month during the first quarter of 2022. Nyxoah expects monthly cash burn to increase slightly
as the year progresses to account for the commencement of the ACCCESS IDE trial in the U.S., and current cash position provides ample
liquidity to get to U.S. commercialization in 2024.
First Quarter 2022 Report
Nyxoah's financial report for the first
quarter of 2022, including details of the consolidated results, are available on the investor page of Nyxoah's website (https://investors.nyxoah.com/financials).
Conference call and webcast presentation
Nyxoah will conduct a conference call open to
the public tomorrow, May 10, 2022, at 2:00 p.m. CET / 8:00 a.m. ET, which will also be webcasted. To participate in the
conference call, please dial one of the following numbers:
USA: (844) 260-3718
Belgium: 0800 73264
International: (929) 517-0938
A question-and-answer session will follow the
presentation of the results. To access the live webcast, go to https://investors.nyxoah.com/events. The archived webcast will
be available for replay shortly after the close of the call.
Nyxoah is a medical technology company focused
on the development and commercialization of innovative solutions to treat Obstructive Sleep Apnea (OSA). Nyxoah's lead solution
is the Genio system, a patient-centered, leadless and battery-free hypoglossal neurostimulation therapy for OSA, the
world's most common sleep disordered breathing condition that is associated with increased mortality risk and cardiovascular comorbidities.
Nyxoah is driven by the vision that OSA patients should enjoy restful nights and feel enabled to live their life to its fullest.
Following the successful completion of the BLAST
OSA study, the Genio system received its European CE Mark in 2019. Nyxoah completed two successful IPOs: on Euronext
Brussels in September 2020 and NASDAQ in July 2021. Following the positive outcomes of the BETTER SLEEP study, Nyxoah received
CE mark approval for the expansion of its therapeutic indications to Complete Concentric Collapse (CCC) patients, currently contraindicated
in competitors' therapy. Additionally, the Company is currently conducting the DREAM IDE pivotal study for FDA and US commercialization
more information, please visit http://www.nyxoah.com/.
- CE marked since 2019. Investigational device in the United States. Limited by U.S. federal law to investigational use
in the United States.
Forward-looking statements
Certain statements, beliefs and opinions in this
press release are forward-looking, which reflect the Company's or, as appropriate, the Company directors' or managements' current expectations
regarding the Genio system; planned and ongoing clinical studies of the Genio system; the potential advantages
of the Genio system; Nyxoah's goals with respect to the development, regulatory pathway and potential use of the
Genio system; the utility of clinical data in potentially obtaining FDA approval of the Genio system;
and the Company's results of operations, financial condition, liquidity, performance, prospects, growth and strategies. By their nature,
forward-looking statements involve a number of risks, uncertainties, assumptions and other factors that could cause actual results or
events to differ materially from those expressed or implied by the forward-looking statements. These risks, uncertainties, assumptions
and factors could adversely affect the outcome and financial effects of the plans and events described herein. Additionally, these risks
and uncertainties include, but are not limited to, the risks and uncertainties set forth in the "Risk Factors" section of
the Company's Annual Report on Form 20-F for the year ended December 31, 2021, to be filed with the Securities and Exchange
Commission ("SEC") on March 24, 2022, and subsequent reports that the Company files with the SEC. A multitude of factors
including, but not limited to, changes in demand, competition and technology, can cause actual events, performance or results to differ
significantly from any anticipated development. Forward looking statements contained in this press release regarding past trends or activities
Last updated: May 10, 2022